Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay

Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China

(2015) Shi-Hong Duan et al.   ACTA OTO-LARYNGOLOGICA

Deafness Gene Variations in a 1120 Nonsyndromic Hearing Loss Cohort

(2015) Shin-ya Nishio et al.   ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY

GJB2 as Well as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness

(2015) Yuan Fang et al.   CELL BIOCHEMISTRY AND BIOPHYSICS

The Prevalence of Gap Junction Protein Beta 2 (GJB2) Mutations in Non Syndromic Sensorineural Hearing Loss in Çukurova Region

(2015) Sevcan Tug Bozdogan et al.   Journal of International Advanced Otology

Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China

(2015) Yi Jiang et al.   PLoS One

Identification of a novel missense mutation in theWFS1gene as a cause of autosomal dominant nonsyndromic sensorineural hearing loss in all-frequencies

(2014) Xiaohui Bai et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss

(2014) Wan Du et al.   GENOMICS

Interleukin 1B rs16944 G>A polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population

(2013) Liang Zheng et al.   CLINICAL BIOCHEMISTRY

MiR-196a2 rs11614913 T>C polymorphism and risk of esophageal cancer in a Chinese population

(2013) Jishu Wei et al.   HUMAN IMMUNOLOGY

Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China

(2013) Feng Xin et al.   Journal of Translational Medicine

Subgroups of enlarged vestibular aqueduct in relation toSLC26A4mutations and hearing loss

(2013) Yasuhide Okamoto et al.   LARYNGOSCOPE

Genome-wide association study validation identifies novel loci for atherosclerotic cardiovascular disease

(2012) X. CHEN et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Identification of Allelic Variants of Pendrin (SLC26A4) with Loss and Gain of Function

(2011) Silvia Dossena et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct

(2011) Shasha Huang et al.   Journal of Translational Medicine

Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes

(2009) B Y Choi et al.   JOURNAL OF MEDICAL GENETICS

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

(2009) Yongyi Yuan et al.   Journal of Translational Medicine

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

(2009) Pu Dai et al.   Journal of Translational Medicine

SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

(2008) Pu Dai et al.   GENETICS IN MEDICINE

Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population

(2008) Sung-Hee Han et al.   JOURNAL OF HUMAN GENETICS